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Studies of the protonation equilibria of sulphamates using 13C and 1C nuclear magnetic resonance spectroscopic, potentiometric, and conductimetric methods

  • William J. Spillane
  • , James B. Thomson
  • University College Dublin

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

10 Citations (Scopus)

Abstract

pKa Values are determined for the ionization RNH2SO3⇌RNHSO3- + H+ for sulphamates with R = Bun, PrnBua, and cyclohexyl using13C and 1H n.m.r. spectroscopic, potentiometric. and conductimetric methods. These compounds have pKa values in the range 1-1.9 and they are thus less acidic than sulphamic acid. Intramolecular standards were used in the n.m.r. measurements. The similarity in the pKa values determined by the two n.m.r. methods suggests that solvation effects are small.

Original languageEnglish
Pages (from-to)580-584
Number of pages5
JournalJournal of the Chemical Society. Perkin Transactions 2
Issue number5
DOIs
Publication statusPublished - 1977

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